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Structure of 28279-49-4
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6-Bromo-4H-imidazo[4,5-b]pyridine serves as a versatile heterocyclic scaffold for medicinal chemistry and materials synthesis. The bromine substituent enables direct functionalization via cross-coupling reactions, while the fused imidazopyridine core provides rigidity and electron-deficient character suitable for targeted molecular design. This compound features high thermal stability and compatibility with standard reaction conditions.
6-Bromo-4H-imidazo[4,5-b]pyridine serves as a versatile building block for heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its well-defined electrophilic bromine site. The imidazopyridine core exhibits robust bench stability and functional group tolerance, facilitating integration into complex scaffolds relevant to medicinal chemistry. Its reactivity profile supports efficient construction of fused polycyclic systems and API intermediates under standard coupling conditions.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: